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Sign in to claim this brandNORTH AMERICAN RESCUE, LLC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 35 TEDWALL COURT, Greer, SC, 29650
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005034064
- DUNS Number
- —
Catalogue (3581)
Page 64 of 72| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nar | 85-4489 | FDA UDI | Class I | Active |
| NAR Kit | 80-1109 | FDA UDI | N/A | Active |
| NAR Kit | ZZ-0423 | FDA UDI | Class I | Active |
| Nar | 85-2020 | FDA UDI | N/A | Active |
| Nar | 85-4301 | FDA UDI | Class I | Active |
| Nar | 80-1582 | FDA UDI | N/A | Active |
| Nar | 77-0080 | FDA UDI | Class I | Active |
| NAR Kit | 85-3206 | FDA UDI | N/A | Active |
| Nar | 85-2963 | FDA UDI | N/A | Active |
| Nar | 85-3513 | FDA UDI | N/A | Active |
| Nar | 85-2669 | FDA UDI | N/A | Active |
| Nar | 85-2125 | FDA UDI | N/A | Active |
| Nar | 85-3929 | FDA UDI | N/A | Active |
| Nar | 85-3347 | FDA UDI | N/A | Active |
| Nar | 85-4435 | FDA UDI | Class I | Active |
| Nar | 85-4173 | FDA UDI | N/A | Active |
| Nar | 85-2131 | FDA UDI | N/A | Active |
| Nar | 80-1728 | FDA UDI | Class I | Active |
| Nar | 85-2094 | FDA UDI | N/A | Active |
| Nar | 85-1736 | FDA UDI | N/A | Active |
| NAR Kit | 85-2761 | FDA UDI | N/A | Active |
| Nar | 85-4299 | FDA UDI | Class I | Active |
| Nar | 80-1763 | FDA UDI | Class I | Active |
| Nar | 85-3076 | FDA UDI | N/A | Active |
| Nar | 85-4588 | FDA UDI | Class I | Active |
| Nar | 85-4422 | FDA UDI | Class I | Active |
| Nar | ZZ-0056 | FDA UDI | Class I | Active |
| Nar | 80-1006 | FDA UDI | N/A | Active |
| NAR Kit | 70-0006 | FDA UDI | N/A | Unknown |
| Nar | 85-4067 | FDA UDI | N/A | Active |
| Nar | 85-4918 | FDA UDI | N | Active |
| NAR Kit | 85-3345 | FDA UDI | N/A | Active |
| Nar | 88-0011 | FDA UDI | Class I | Active |
| Nar | 85-3939 | FDA UDI | N/A | Active |
| Nar | 85-3087 | FDA UDI | N/A | Active |
| Nar | 85-1123 | FDA UDI | N/A | Active |
| Nar | 85-1685 | FDA UDI | N/A | Active |
| NAR Kit | 85-1762 | FDA UDI | N/A | Unknown |
| NAR Kit | 85-3637 | FDA UDI | N/A | Active |
| Nar | 85-1815 | FDA UDI | N/A | Active |
| Nar | 80-0953 | FDA UDI | N/A | Active |
| NAR Kit | 85-0014 | FDA UDI | N/A | Active |
| Nar | 80-1066 | FDA UDI | N/A | Active |
| Nar | 85-3400 | FDA UDI | N/A | Active |
| Nar | 85-2319 | FDA UDI | Class I | Active |
| NAR Kit | 85-1185 | FDA UDI | N/A | Active |
| Nar | 85-4057 | FDA UDI | N/A | Active |
| Nar | 85-3867 | FDA UDI | N/A | Active |
| Nar | 85-4110 | FDA UDI | N/A | Active |
| NAR Kit | 85-3291 | FDA UDI | N/A | Active |
Related Companies
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Importers
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Notified Bodies
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Authorities
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FDA Recalls (4)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Mar 27, 2026 | Z-1947-2026 | — | open, classified | Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the meter displays an E-5 error code for a very high blood glucose event (> 600 mg/dL) or when there is a test strip error, which can lead to operator confusion when evaluating patients and a delay in appropriate treatment. This is a downstream recall of Trividia Health Class I, Recall Event ID 98317. |
| Jul 1, 2025 | Z-2637-2025 | — | open, classified | Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use. |
| Aug 27, 2021 | Z-2520-2021 | — | terminated | The device includes the incorrect Instructions for Use. |
| Aug 21, 2020 | Z-3018-2020 | — | terminated | Lack of sterility assurance of the 30-0171 |